Interpreting aCGH-defined karyotypic changes in gliomas using copy number status, loss of heterozygosity and allelic ratios

Exp Mol Pathol. 2010 Feb;88(1):82-9. doi: 10.1016/j.yexmp.2009.09.014. Epub 2009 Oct 7.

Abstract

We have used SNP mapping arrays to simultaneously record copy number changes, loss of heterozygosity and allele ratios (ploidy) in a series of 13 gliomas. This combined analysis has defined novel amplification events in this tumor type involving chr1:241544532-243005121 and chr18:54716681-54917277 which contain the AKT3 and ZNF532 genes, respectively. The high resolution of this analysis has also identified homozygous deletions involving chr17:25600031-26490848 and Chr19:53883612-55061878. Throughout the karyotypes of these tumors, the combined analysis revealed counter intuitive relationships between copy number and LOH that requires reinterpretation of the significance of copy number gains and losses. It was not uncommon to observe copy number gains that were associated with loss of heterozygosity as well as copy number losses that were not. These events appeared to be related to ploidy status in the tumors as determined using allelic ratio calculations. Overall, this analysis of gliomas provides evidence for the need to perform more comprehensive interpretation of the CGH data beyond copy number analysis alone to evaluate the significance of individual events in the karyotypes.

MeSH terms

  • Aneuploidy
  • Chromosome Mapping / methods
  • Comparative Genomic Hybridization / methods*
  • DNA Copy Number Variations*
  • DNA, Neoplasm / analysis
  • Gene Deletion
  • Glioma / genetics*
  • Glioma / metabolism
  • Glioma / pathology
  • Humans
  • Loss of Heterozygosity*
  • Oligonucleotide Array Sequence Analysis
  • Polymorphism, Single Nucleotide*

Substances

  • DNA, Neoplasm